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在原发性心血管预防中,患有白蛋白尿的 2 型糖尿病患者的非目标风险因素数量与心血管风险相关。NID-2 试验的事后分析。

The number of risk factors not at target is associated with cardiovascular risk in a type 2 diabetic population with albuminuria in primary cardiovascular prevention. Post-hoc analysis of the NID-2 trial.

机构信息

Department of Advanced Medical and Surgical Sciences, University of Campania "Luigi Vanvitelli", Piazza Luigi Miraglia 2, 80138, Naples, Italy.

Department of Physical and Mental Health and Preventive Medicine, Medical Statistics Unit, University of Campania "Luigi Vanvitelli", Piazza Luigi Miraglia 2, 80138, Naples, Italy.

出版信息

Cardiovasc Diabetol. 2022 Nov 7;21(1):235. doi: 10.1186/s12933-022-01674-7.

Abstract

BACKGROUND

Nephropathy in Diabetes type 2 (NID-2) study is an open-label cluster randomized clinical trial that demonstrated that multifactorial intensive treatment reduces Major Adverse Cardiac Events (MACEs) and overall mortality versus standard of care in type 2 diabetic subjects with albuminuria and no history of cardiovascular disease. Aim of the present post-hoc analysis of NID- 2 study is to evaluate whether the number of risk factors on target associates with patient outcomes.

METHODS

Intervention phase lasted four years and subsequent follow up for survival lasted 10 years. To the aim of this post-hoc analysis, the whole population has been divided into 3 risk groups: 0-1 risk factor (absent/low); 2-3 risk factors (intermediate); 4 risk factors (high). Primary endpoint was a composite of fatal and non-fatal MACEs, the secondary endpoint was all-cause death at the end of the follow-up phase.

RESULTS

Absent/low risk group included 166 patients (52.4%), intermediate risk group 128 (40.4%) and high-risk group 23 (7.3%). Cox model showed a significant higher risk of MACE and death in the high-risk group after adjustment for confounding variables, including treatment arm (HR 1.91, 95% CI 1.04-3.52, P = 0.038 and 1.96, 95%CI 1.02-3.8, P = 0,045, respectively, vs absent/low risk group).

CONCLUSIONS

This post-hoc analysis of the NID-2 trial indicates that the increase in the number of risk factors at target correlates with better cardiovascular-free survival in patients with type 2 diabetes at high CV risk.

CLINICAL TRIAL REGISTRATION

ClinicalTrials.gov number, NCT00535925. https://clinicaltrials.gov/ct2/show/NCT00535925.

摘要

背景

2 型糖尿病肾病(NID-2)研究是一项开放性标签的聚类随机临床试验,该研究表明,在有蛋白尿且无心血管疾病史的 2 型糖尿病患者中,多因素强化治疗可降低主要不良心脏事件(MACEs)和整体死亡率,优于标准治疗。本 NID-2 研究的事后分析旨在评估目标风险因素的数量是否与患者结局相关。

方法

干预阶段持续 4 年,随后对生存情况进行了 10 年的随访。为了进行本事后分析,将整个研究人群分为 3 个风险组:0-1 个风险因素(缺失/低);2-3 个风险因素(中);4 个风险因素(高)。主要终点是致命性和非致命性 MACE 的复合终点,次要终点是随访结束时的全因死亡。

结果

缺失/低风险组包括 166 例患者(52.4%),中风险组 128 例(40.4%),高风险组 23 例(7.3%)。Cox 模型显示,在校正混杂因素(包括治疗分组)后,高风险组的 MACE 和死亡风险显著升高(HR 1.91,95%CI 1.04-3.52,P=0.038 和 1.96,95%CI 1.02-3.8,P=0.045,分别与缺失/低风险组相比)。

结论

本 NID-2 试验的事后分析表明,目标风险因素数量的增加与高心血管风险的 2 型糖尿病患者的心血管无事件生存率的改善相关。

临床试验注册

ClinicalTrials.gov 编号,NCT00535925。https://clinicaltrials.gov/ct2/show/NCT00535925。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b747/9641842/b27c3d03cfc4/12933_2022_1674_Fig1_HTML.jpg

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